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黄芪多糖通过调节FoxO3a/Wnt信号通路对去卵巢大鼠骨质疏松症的抑制作用

Inhibitory effect of Astragalus polysaccharide on osteoporosis in ovariectomized rats by regulating FoxO3a /Wnt signaling pathway.

作者信息

Ou Li, Wei Peifeng, Li Min, Gao Feng

机构信息

Department of Clinical Chinese Pharmacy, College of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, China.

出版信息

Acta Cir Bras. 2019;34(5):e201900502. doi: 10.1590/s0102-865020190050000002. Epub 2019 Jun 3.

Abstract

PURPOSE

To investigate inhibitory effect of Astragalus polysaccharide (APS) on osteoporosis in ovariectomized rats by regulating FoxO3a/Wnt2 signaling pathway.

METHODS

Postmenopausal osteoporosis (PMOP) animal model was developed by excising the bilateral ovaries of rats. The model rats were administered with APS (200 mg/kg, 400 mg/kg, 800 mg/kg) by intragastric administration once daily for 12 weeks. Bone density, bone metabolism index and oxidative stress index were measured in all groups. Furthermore, the regulation of APS of FoxO3a / Wnt2 signaling pathway was observed.

RESULTS

APS has an estrogen-like effect, which can increase bone mass, lower serum ALP and BGP values, increase blood calcium content, and increase bone density of the femur and vertebrae in rats. At the same time, APS can increase the bone mineral content of the femur, increase the maximum stress, maximum load and elastic modulus of the ovariectomized rats, improve oxidative stress in rats by increasing the gene expression of β-catenin and Wnt2 mRNA and inhibiting the gene expression of FoxO3a mRNA.

CONCLUSION

Astragalus polysaccharide can effectively alleviate oxidative stress-mediated osteoporosis in ovariectomized rats, which may be related to its regulation of FoxO3a/Wnt2/β-catenin pathway.

摘要

目的

通过调节FoxO3a/Wnt2信号通路,研究黄芪多糖(APS)对去卵巢大鼠骨质疏松症的抑制作用。

方法

通过切除大鼠双侧卵巢建立绝经后骨质疏松症(PMOP)动物模型。对模型大鼠每日灌胃给予APS(200mg/kg、400mg/kg、800mg/kg),持续12周。检测所有组的骨密度、骨代谢指标和氧化应激指标。此外,观察APS对FoxO3a / Wnt2信号通路的调节作用。

结果

APS具有类雌激素作用,可增加大鼠骨量,降低血清碱性磷酸酶(ALP)和骨钙素(BGP)值,提高血钙含量,增加大鼠股骨和椎骨的骨密度。同时,APS可增加股骨骨矿物质含量,提高去卵巢大鼠的最大应力、最大负荷和弹性模量,通过增加β-连环蛋白基因表达和Wnt2 mRNA,抑制FoxO3a mRNA基因表达来改善大鼠氧化应激。

结论

黄芪多糖可有效减轻去卵巢大鼠氧化应激介导的骨质疏松症,这可能与其对FoxO3a/Wnt2/β-连环蛋白通路的调节有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b2f/6583917/f70eb0ce4bb2/1678-2674-acb-34-05-e201900502-gf1.jpg

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